Electrical stimulation of ilioinguinal nerve to alleviate chronic pelvic pain

ABSTRACT

The disclosure describes a method and system for applying electrical stimulation to an ilioinguinal nerve of a patient. The system includes electrical stimulators that apply electrical stimulation for alleviation of pelvic pain. The system may apply electrical stimulation for pelvic pain in men or women. The electrical stimulators may comprise various types of electrodes such as cuff electrodes, electrode leads, and microstimulators implanted at various locations proximate to a single or both ilioinguinal nerves of a patient. In particular, the electrode may be implanted proximate or adjacent to a region of the ilioinguinal nerve above or below the inguinal canal.

TECHNICAL FIELD

The invention relates to medical devices and, more particularly, to devices for delivering neurostimulation therapy.

BACKGROUND

Pain in the pelvic region, including urogenital pain, may be caused by a variety of injuries or disorders in men and women. For example, ilioinguinal neuralgia, iliohypogastric neuralgia, genitofemoral neuralgia, chronic groin pain, chronic testicular pain (CTP), post vasectomy pain, and other pain originating from the testicles, groin, or abdomen are common reasons for referral to a urological specialist.

As an example, ilioinguinal, iliohypogastric, and genitofemoral neuralgia may be attributed to nerve injury, such as stretching of a nerve, electrocoagulation, stricture caused by ligation, entrapment of the nerve in scar tissue, or irritation because of proximity to a zone of inflammation, during inguinal hemiorrhaphy. In addition to hemiorrhaphy, other abdominal procedures that may cause these neuralgias or CTP include appendectomy, iliac crest bone graft harvesting, urological operations, and gynecological surgery, including transverse or paramedian incisions for hysterectomy. The pain experienced by the patient may be unilateral or bilateral, constant or intermittent, spontaneous or exacerbated by physical activities and pressure, and may remain localized in the scrotum or radiate to the groin, perineum, back, or legs.

Typically, denervation procedures are used to treat various neuralgias. In denervation procedures, the nerve that is diagnosed as the cause, e.g., using the results of the patient history, physical examination, preoperative electromyography, and nerve blocks, is severed or permanently removed. Such procedures may result in permanent and substantial pain relief regardless of the origin of pain. However, severing or removing some nerves may result in loss of sensation. Therapeutic nerve blocks may also be used to treat various neuralgias, but generally only relieve pain temporarily.

In addition, women may experience various types of sources of pelvic pain. Sources of pain may include injury to nerves resulting from surgical procedures, non-surgical conditions, vulvodynia which can be very debilitating but has no obvious source, and interstitial cystitis (painful bladder syndrome). Interstitial cystitis may be a source of pelvic pain in both women and men. Surgical procedures that may injure nerves in the pelvic region may include urological operations in the pelvic area, gynecological surgery, and hysterectomy. Non-surgical conditions which cause pain in women include adhesions, endometriosis, and pelvic congestion.

SUMMARY

In general, the invention is directed to techniques for applying electrical stimulation to an ilioinguinal nerve of a patient via an implantable electrical stimulation device to alleviate symptoms of chronic pelvic pain in men or women. Pelvic pain may include urogenital pain or other forms of pelvic pain. The electrical stimulation may be applied to one or both ilioinguinal nerves.

A system according to the invention may include one or more electrical stimulators that apply electrical stimulation to the ilioinguinal nerve to alleviate chronic groin pain or other afflictions associated with pelvic pain, including pain originating from the testicles, groin, or abdomen, such as post vasectomy pain and ilioinguinal neuralgia. In female patients, an electrical stimulator delivers the stimulation to the ilioinguinal nerve to alleviate other types of pelvic pain such as vulvodynia, interstitial cystitis, post-operative pain, adhesions, endometriosis or pelvic congestion.

The electrical stimulators may comprise various types of electrodes such as cuff electrodes, electrode leads, and/or microstimulators implanted at various locations proximate to one or both of the ilioinguinal nerves of a patient. In particular, the electrical stimulators may be implanted proximate to one or both ilioinguinal nerves above or below the inguinal canal. Stimulation may be applied uni-laterally, i.e., via a single ilioinguinal nerve, or bi-laterally, i.e., via both ilioinguinal nerves.

In some embodiments, electrical stimulation electrodes may be coupled to an implantable stimulation device implanted within a subcutaneous pocket in the abdomen of the patient or, alternatively, the scrotum or buttock of the patient. The electrical stimulation electrodes may be coupled to the implantable medical device via standard implantable electrode leads. Alternatively, leadless microstimulators may be positioned adjacent the target nerves. In this case, the leadless microstimulators may be capable of wireless communication with other implantable medical devices, an external programmer, or both.

For male patients, stimulation electrodes or leadless microstimulators may be implanted using well known surgical procedures such as those used in repairing an inguinal hernia, exposing the spermatic cord, or ilioinguinal denervation. Systems including such electrodes or microstimulators and employing the techniques described in this disclosure may substantially reduce or eliminate chronic pelvic pain, including urogenital pain such as chronic groin pain or ilioinguinal neuralgia, without loss of sensation in the skin of the superomedial thigh, the root of the penis, and/or scrotum as is common with ilioinguinal nerve and spermatic cord denervation procedures.

Systems according to the invention may include an external programmer that programs the electrical stimulators to apply electrical stimulation to an ilioinguinal nerve. During stimulation, a clinician or patient may operate the external programmer to adjust stimulation parameters, such as amplitude, pulse width, pulse rate, and electrode polarities. In some cases, a patient may use the programmer to deliver stimulation on demand, e.g., when the patient experiences discomfort. Additionally or alternatively, the implantable stimulation device may store stimulation programs and schedules. In this manner, the electrical stimulation can be delivered according to preprogrammed stimulation parameters and schedules, if desired.

In one embodiment, the invention provides a method comprising applying electrical stimulation to an ilioinguinal nerve of a patient via an implanted electrical stimulation device.

In another embodiment, the invention provides a system comprising an implantable electrical stimulation device that generates electrical stimulation selected to alleviate pelvic pain, and an electrode coupled to the electrical stimulation device at a position adjacent to an ilioinguinal nerve of a patient.

In a further embodiment, the invention provides a method comprising applying electrical stimulation to at least a portion of an ilioinguinal nerve of a patient via an implanted electrical stimulation device.

In another embodiment, the invention provides a system comprising an implantable electrical stimulation device that generates electrical stimulation selected to alleviate pelvic pain, and an electrode coupled to the electrical stimulation device at a position adjacent to an ilioinguinal nerve of a patient.

In various embodiments, the invention may provide one or more advantages. For example, applying electrical stimulation to an ilioinguinal nerve of a patient may substantially reduce or eliminate pelvic pain such as that caused by chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term pain in the testicles, groin, or abdomen, as well as other forms of pelvic pain experienced by female patients.

Ilioinguinal denervation procedures that sever or remove the ilioinguinal nerve often result in unwanted side effects including loss of sensation in the skin of the superomedial thigh, the root of the penis, and/or scrotum. Therapeutic nerve blocks typically only relieve pain temporarily. In contrast, delivery of electrical stimulation to one or both ilioinguinal nerves may provide permanent or long-lived effective therapy for many patients with fewer or no unwanted side effects.

In addition, for male patients, electrical stimulators may be implanted proximate to the ilioinguinal nerve using well known surgical procedures for repairing an inguinal hernia, exposing the spermatic cord, or ilioinguinal denervation, thereby providing ease of deployment by experienced surgeons or other caregivers.

The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic diagram illustrating an example system that includes an implantable stimulation device for applying electrical stimulation to an ilioinguinal nerve of a patient for alleviation of pelvic pain from a front view of a male patient.

FIG. 2 is a schematic diagram further illustrating the example system of FIG. 1 from a side view of a male patient.

FIGS. 3A, 3B and 3C are schematic diagrams illustrating an example cuff electrode useful in the system of FIGS. 1 and 2.

FIG. 4 is a block diagram illustrating an example implantable stimulation device for applying electrical stimulation to the ilioinguinal nerve of a patient.

FIG. 5 is a block diagram illustrating an example clinician programmer that allows a clinician to program electrical stimulation therapy for a patient.

FIG. 6 is a schematic diagram illustrating another example system including two different types of electrical stimulators for applying electrical stimulation to an ilioinguinal nerve of a patient from a front view of a male patient.

FIG. 7 is a schematic diagram further illustrating the example system of FIG. 6 from a side view of a male patient.

FIGS. 8A and 8B are schematic diagrams illustrating an example electrode lead of FIGS. 6 and 7.

FIG. 9 is a schematic diagram further illustrating the example system of FIG. 6.

FIGS. 10A, 10B and 10C are schematic diagrams illustrating an example leadless microstimulator suitable for use in the system of FIGS. 6 and 7.

FIG. 11 is a side cross-sectional view of a leadless electrical microstimulator implanted within tissue proximate to the ilioinguinal nerve of a patient.

FIG. 12 is a schematic diagram illustrating implantation of a leadless microstimulator within tissue proximate to the ilioinguinal nerve.

FIG. 13 is a functional block diagram illustrating various components of the leadless microstimulator of FIG. 11.

FIG. 14 is a schematic diagram illustrating another configuration for the example system of FIG. 7.

FIG. 15 is a flow chart illustrating a technique for applying electrical stimulation to an ilioinguinal nerve of a patient for alleviation of pelvic pain.

DETAILED DESCRIPTION

FIG. 1 is a schematic diagram illustrating an example system 2 that includes an implantable medical device (IMD) 28 in the form of an electrical stimulator that applies electrical stimulation to one or both ilioinguinal nerves of a patient 10. In FIG. 1, system 2 is illustrated from a front view perspective of patient 10. Although the invention may be generally applicable to treat pelvic pain in both men and women, application of the invention to men will be described throughout this disclosure for purposes of illustration. Throughout the figures accompanying this disclosure, various anatomical features of patient 10 and structural features of system 2 are illustrated conceptually for ease of illustration. Accordingly, the figures may not necessarily present appropriate scales and proportions of such anatomical features. Rather, the drawings are provided as a conceptual rendering of such features to aid in the understanding of pertinent embodiments of the invention.

In the example of FIG. 1, IMD 28 applies electrical stimulation to patient 10 for alleviation of chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, or other conditions that cause long term (chronic) pain in the testicles (in a male patient), groin, or abdomen. As an example, chronic groin pain may be attributed to nerve injury, such as stretching of a nerve, electrocoagulation, stricture caused by ligation, entrapment of the nerve in scar tissue, or irritation proximate to a zone of inflammation, during inguinal hemiorrhaphy or other previous surgical interventions. In addition to hemiorrhaphy, other abdominal procedures that may cause chronic groin pain or ilioinguinal neuralgia include appendectomy, iliac crest bone graft harvesting, urological operations, and gynecological surgery, including transverse or paramedian incisions for hysterectomy. In particular, damage to the ilioinguinal nerve may cause a patient to experience pain in the skin of the superomedial thigh, the root of the penis, and/or associated scrotal area. IMD 28 may also deliver stimulation to patient 10 for alleviation of chronic pelvic pain that is idiopathic in origin. Stimulation parameters such as amplitude, pulse width and pulse rate may be selected as appropriate to alleviate pain for the particular patient 10.

In additional embodiments, IMD 28 applies electrical stimulation to a female patient (not shown) for alleviation of pelvic pain such as, urogenital pain and idiopathic pain. Examples of pain include pain resulting from surgical procedures, non-surgical procedures, vulvodynia, and interstitial cystitis (painful bladder syndrome). Nerve injury may be caused by various surgical procedures including urological operations in the pelvic area, gynecological surgery, and hysterectomy. Non-surgical conditions which cause pain in women include adhesions, endometriosis, and pelvic congestion. Applying electrical stimulation to the ilioinguinal nerve in accordance with selected stimulation parameters may alleviate pain experienced by female patients.

FIG. 1 illustrates ilioinguinal nerves 30, 31, iliohypogastric nerves 32, 33, genital branches 22, 23 and femoral branches 24, 25 of genitofemoral nerves 20, 21, respectively. Spermatic cords 14, 15 include a portion of genital branches 22, 23 of genitofemoral nerves 20, 21, respectively. Generally, IMD 28 delivers electrical stimulation to ilioinguinal nerves 30, 31 via electrodes which may be coupled to IMD 28 by one or more leads. The electrical stimulation has parameters selected to block pain signals from the superomedial region of thighs 6, 7, penis 8, testicles 12, 13, and/or the associated scrotal area 11 from reaching the central nervous system (CNS). The electrodes may be configured to at least partially engage a portion of ilioinguinal nerves 30, 31 or may be implanted proximate to ilioinguinal nerves 30,31.

More specifically, as shown in the example of FIG. 1, electrodes may be implanted proximate to a portion of ilioinguinal nerves 30, 31 above or superior to inguinal canals 26, 27 or a portion of ilioinguinal nerves 30, 31 below or above inguinal canals 26, 27. For example, electrodes may be implanted proximate to a region of ilioinguinal nerve 30 above inguinal canal 26 or a portion of ilioinguinal nerve 30 below inguinal canal 26. In another example, electrodes may be implanted proximate to a region of ilioinguinal nerve 30 above inguinal canal 26 and a portion of ilioinguinal nerve 30 below inguinal canal 26. The invention further includes embodiments in which electrodes are implanted bi-laterally in any combination. Such embodiments are included without exhaustively listing all possible combinations. Accordingly, the positions of electrodes 16 and 17 in FIG. 1 is merely exemplary.

The pain experienced by the patient may be unilateral or bilateral, constant or intermittent, spontaneous or exacerbated by physical activities and pressure, and may remain localized or radiate outward. In a male patient, for example, pain may remain localized in the penis, or radiate to the scrotum, thighs, perineum, or back. Delivering electrical stimulation may cause parasthesia in penis 8, thighs 6, 7, testicles 12 and 13 and associated scrotal region 11 based on the position of the electrodes. The number and position of the leads may be dependent on the pain perceived by the patient and the type of electrical stimulation delivered to treat the pain.

In the illustrated example, IMD 28 is coupled to leads 18 and 19. Leads 18 and 19 each include a cuff electrode, i.e., cuff electrodes 16 and 17, that delivers electrical stimulation therapy to ilioinguinal nerves 30 and 31, respectively. A cuff electrode includes a cuff-like fixation structure and one or more electrodes carried by the fixation structure. In the example of FIG. 1, leads 18 and 19 are implanted at different locations along ilioinguinal nerves 30 and 31, respectively. As a result, patient 10 may experience paresthesia in different areas on each side of his body in response to electrical stimulation delivered by electrodes 16 and 17.

Although cuff electrodes are shown in FIG. 1, the leads coupled to IMD 28 may include various types of electrodes depending on the type of stimulation delivered and the location of the lead. For example, IMD 28 may be coupled to any number and any type of electrodes, such as conventional ring electrode leads, paddle electrode leads, and other electrodes suitable for delivering electrical stimulation to ilioinguinal nerves 30, 31. In addition, in some cases, leadless stimulators may be used. A cuff electrode may provide more direct electrical contact, i.e., better electrical coupling, with an ilioinguinal nerve than a standard electrode lead. However, in some cases, applying electrical stimulation directly to a nerve may result in the patient experiencing an unpleasant sensation, such as a burning sensation. Consequently, a standard electrode implanted proximate to the ilioinguinal nerve lead may be advantageous because the patient may experience a more pleasant paresthesia as a result of stimulation. In addition, a standard electrode lead may also be advantageous in terms of surgical ease.

As an example, FIG. 6 illustrates another system in which an IMD is coupled to an electrode lead having electrodes on the distal end of the lead to stimulate an ilioinguinal nerve of a patient. FIG. 6 also illustrates a leadless microstimulator implanted within the tissue adjacent to the ilioinguinal nerve. In this case, an IMD or external programmer may wirelessly control the leadless microstimulator to deliver electrical stimulation to the adjacent tissue. In addition, although not illustrated, an IMD may also be coupled to an electrode suitable for applying electrical stimulation to genital branches 22, 23 and/or femoral branches 24, 25, of genitofemoral nerves 20, 21 or iliohypogastric nerves 32, 33.

With further reference to FIG. 1, IMD 28 may be coupled to deliver electrical stimulation energy to ilioinguinal nerves 30, 31 via cuff electrodes 16, 17, respectively. Cuff electrodes 16 and 17 each may comprise a rigid or flexible cuff electrode, a self-sizing spiral cuff electrode, a half cuff electrode, a helical electrode, a chambered electrode, or other types of cuff electrodes that are shaped, sized and otherwise configured to at least partially wrap around an ilioinguinal nerve. The cuff electrode may be sized and shaped to at least partially enclose the ilioinguinal nerve and promote electrical coupling pressure between the electrode and the ilioinguinal nerve. The cuff electrodes 16, 17 may each include a single electrode or multiple electrodes. For example, a cuff electrode 16, 17 may include a bipolar or multipolar arrangement of electrodes or a unipolar electrode that is referenced to the electrical potential of an active can electrode carried by IMD 28.

IMD 28 includes electrical stimulation pulse generator circuitry and delivers electrical stimulation in the form of electrical pulses in accordance with stored stimulation parameters, e.g., electrode combination, electrode polarity, pulse amplitudes, pulse widths, pulse rates, and/or duty cycle. By way of example, the electrical stimulation may include stimulation pulses having pulse widths between approximately 10 and 5000 microseconds, more preferably between approximately 100 and 1000 microseconds, and still more preferably between 180 and 450 microseconds. The stimulation pulses may define voltage amplitudes between approximately 0.1 and 50 volts, more preferably between approximately 0.5 and 20 volts, and still more preferably between approximately 1 and 10 volts. The pulses may have frequencies between approximately 0.5 and 500 hertz, more preferably between approximately 10 and 250 hertz, and still more preferably between approximately 50 and 150 hertz. The pulses may be alternating current (ac) pulses or direct current (dc) pulses, and may be mono-phasic, bi-phasic, or multi-phasic in various embodiments.

IMD 28 may drive electrodes 16 and 17 with the same or different stimulation pulses or waveforms. In some embodiments, IMD 28 may cause electrodes 16 and 17 to deliver electrical stimulation simultaneously, or in an interleaved or alternating fashion. For example, electrodes 16 and 17 may deliver electrical stimulation with different pulse rates, duty cycles or scheduled times for delivery, which may result in alternating delivery of stimulation. Interleaved or alternating delivery of stimulation may, for example, reduce the likelihood that neural accommodation or tolerance will impair the efficacy of the stimulation. Interleaved or alternating delivery of stimulation may also result in more complete pain relief than would be possible through delivery of stimulation via only one electrode or electrode array. Interleaved stimulation may be delivered via conventional ring electrodes, paddle lead electrodes, cuff electrodes, microstimulators, or the like.

Leads 18 and 19 may be implanted proximate to ilioinguinal nerves 30, 31, respectively. In the illustrated example, lead 18 is implanted proximate to a region of ilioinguinal nerve 30 above inguinal canal 26 and lead 19 is implanted proximate to a region of ilioinguinal nerve 31 below inguinal canal 27, but the invention is not limited as such. Rather, lead 18 may be implanted at various locations along ilioinguinal nerves 30, 31 or sympathetic nerves (not shown). The positions of leads 18 and 19 in FIG. 1 are shown for purposes of illustration to show different possible implantation locations and associated target stimulation sites. Specifically, leads 18 and 19 illustrate two locations which may be particularly advantageous for applying electrical stimulation, which will be described in detail below. However, IMD 28 may be coupled to a single lead or a plurality of leads based on the perceived pain of the patient and his response to electrical stimulation therapy.

The following is a general anatomical description of the ilioinguinal, iliohypogastric, and genitofemoral nerves that may be used for reference. However, the ilioinguinal, iliohypogastric, and geintofemoral nerves have been demonstrated to have a variable origin, course, and distribution in the inguinal region among different patients. In other words, anatomical variability may be observed from patient to patient. Accordingly, the drawings are provided as a conceptual representation to aid in the understanding of pertinent embodiments of the invention, but not necessarily as an accurate anatomical guide.

In FIG. 1, ilioinguinal nerves 30, 31, iliohypogastric nerves 32, 33, and genital branches 22, 23 and femoral branches 24, 25 of genitofemoral nerves 20, 21 are illustrated. FIG. 1 also illustrates inguinal canals 26 and 27. Although not explicitly shown in FIG. 1, the ilioinguinal 30, 31 nerves originate from the L1 and T12 nerves and also, in some cases, the L2 nerve. Generally, the ilioinguinal nerves run subperitoneally below the respective iliohypogastric nerves. The ilioinguinal nerves emerge from the lateral border of the psoas muscle (not shown) and pierce the transverses abdominis muscle (not shown) approximately one centimeter (cm) above the anterior superior iliac spine (not shown) and then cross the internal abdominal oblique muscle (not shown). The ilioinguinal nerves continue beneath the aponeurosis of the external oblique abdominal muscle (not shown) in the direction of the symphysis and pubic region. The ilioinguinal nerves then lie medially, or less frequently, below or lateral to the spermatic cord in men or to the round ligament of the uterus in women and accompany the spermatic cord for approximately two to four centimeters through the respective inguinal canal ring 26, 27. Often, the ilioinguinal nerve has a reciprocal relationship with regard to the diameter of the iliohypogastric nerve. In some cases, branches of the ilioinguinal nerves fan out and innervate the respective spermatic cord. Branches of the ilioinguinal nerves may pierce the oblique muscle aponeurosis to supply the sensory distribution to the skin of the superomedial thigh as well as to the root of the penis and the scrotum in men and to the skin of the mons pubis and labia majora in women.

For reference, the iliohypogastric nerves 32, 33 originate from the anterior branch of the L1 nerve and, frequently, the T12 nerve. The iliohypogastric nerves emerge along the lateral margin of the psoas muscle (not shown) to pass anterior to the quadratus lumborum (not shown). The iliohypogastric nerves perforate the transverses abdominis muscle (not shown) above the iliac crest (not shown) as in the ilioinguinal nerves. Approximately three centimeters to the anterior superior iliac spine, the iliohypogastric nerves may be found between layers of the transversus and internal oblique muscles (not shown). The iliohypogastric nerves divide between the transverus abdominis muscle and the internal oblique muscle into lateral and cutaneous branches.

The lateral cutaneous branch pierces the internal and external oblique muscles. The lateral cutaneous branch is then distributed to the skin of the gluteal region. The anterior cutaneous branch continues between the transverses and internal oblique muscles. The anterior cutaneous branch pierces the internal oblique muscle and becomes cutaneous by perforating the aponeurosis of the external oblique approximately two to three centimeters above the internal ring of the inguinal canal and is distributed to the skin of the hypogastric region, i.e., the skin of the superomedial thigh, root of the penis, testicles, and associated scrotal region.

Genitofemoral nerves 20, 21 originate from the L1 and L2 nerves in the lumbar region (lower back) at L1/L2. As the genitofemoral nerves pass through the lumbar region, the genitofemoral nerves cross behind the ureter (not shown). Slightly posterior to and at a variable distance above the inguinal ligament (not shown), the genitofemoral nerves divide into genital branches and femoral branches. The genital branches cross the transverses abdominus (not shown) and internal oblique muscles (not shown) and enter the respective inguinal canals through the internal inguinal ring.

Within the inguinal canal, genital branches run along the respective spermatic cord. The spermatic cord includes various layers (not shown). These layers are the external spermatic fascia, cremasteric muscle and fascia, ilioinguinal nerve (in some cases), internal spermatic fascia, ductus deferens, lymph vessels, pampiniform plexus of veins which become the testicular vein, and testicular artery. More specifically, as the structures within the spermatic cord pass through the transversalis fascia (not shown), they join with one of the layers of the spermatic cord, the internal spermatic fascia.

In a male patient, as the spermatic cord continues through the inguinal canal, it joins with the cremasteric layer of muscle and fascia from the internal oblique muscle. These muscle fibers perform an important reflex, i.e., the cremasteric reflex. When the cremasteric muscle contracts, the testicle is pulled closer to the body. This reflex keeps the testicles at the correct temperature, for example, by relaxing when the testicles are too warm and contracting when the testicles are too cold.

Finally, when the spermatic cord passes through the superficial ring, it joins an external spermatic fascia layer derived from the aponeurosis of the external oblique. After the spermatic cord traverses the inguinal canal, it leads into the scrotum and to the testes where the genital braches of the genitofemoral nerves innervate the testes.

In accordance with an embodiment of the invention, electrical stimulation may be delivered via electrodes positioned proximate to a region of ilioinguinal nerves 30, 31 superior (above) inguinal canals 26, 27 or positioned proximate to a region of ilioinguinal nerves 30, 31 anterior (below) inguinal canals 26, 27. In the illustrated example, cuff electrode 16 is wrapped around a portion of ilioinguinal nerve 30 above inguinal canal 26 and connected to IMD 28 via lead 18 and, optionally, a lead extension (not shown). The electrical stimulation applied by cuff electrode 16 stimulates ilioinguinal nerve 30.

Electrode 17, in the illustrated example, also comprises a cuff electrode. More specifically, cuff electrode 17 is wrapped around a portion of ilioinguinal nerve 31 below inguinal ring 27. Because cuff electrode 16 is located higher (upstream in the central nervous system) from cuff electrode 17, patient 10 may experience parasthesia over a larger area, which may be advantageous in some instances. However, ilioinguinal nerves 30, 31 may not include an external fascia or other tissue to serve as a protective layer. Consequently, wrapping cuff electrodes 16 and 17 around ilioinguinal nerves 30 and 31 may inherently have a risk of pinching or otherwise damaging the nerve, possibly reducing the long-term efficacy of the electrical stimulation. As a result, care may be necessary when wrapping a cuff electrode around an ilioinguinal nerve.

The positions of electrodes 16, 17 in FIG. 1 are for purposes of illustration of different possible positions. In practice, one or both electrodes 16, 17 may be positioned above inguinal canal 26, 27. Alternatively, one or both electrodes 16, 17 may be positioned below inguinal canal 26, 27. As discussed previously, electrodes may be positioned based on the pain perceived by the patient and the type of electrical stimulation delivered to treat the pain. In general, electrodes may be implanted proximate to a portion of the ilioinguinal nerve above or below the inguinal canal to apply electrical stimulation for treatment of chronic groin pain or ilioinguinal neuralgia.

In general, it may be difficult to wrap a cuff electrode around the ilioinguinal nerve within the inguinal canal. Furthermore, it may not be desirable to apply electrical stimulation to the ilioinguinal nerve within the inguinal canal because of its close proximity to other nerves and/or muscles, e.g., the genital branch of the genitofemoral nerve, cremasteric muscle, and iliohypogastric nerve. Consequently, stimulating the ilioinguinal nerve within the inguinal canal may result in unwanted triggering of the cremasteric reflex.

Leads 18 and 19 are typically either surgically implanted or inserted percutaneously. Leads 18 and 19 may be surgically implanted using well known surgical techniques. For example, the surgical procedure for neurectomy of the ilioinguinal nerve is well defined, i.e., an abdominal incision as used for neurectomy of the ilioinguinal nerve or hernia repair to expose the ilioinguinal and/or iliohypogastric nerve at the point of muscle emergence. A surgical procedure for ilioinguinal and iliohypogastric neurectomy is described in detail in Judith A. Murovic et. al, “Surgical Management of 33 Ilioinguinal and Iliohypogastric Neuralgias at the Louisiana State University Health Sciences Center,” Neurosurgery, Volume 56, Number 5, pages 1013-1020, May 2005. Prior to surgically implanting electrodes, local nerve blocks may be performed using a nerve blocking agent to determine the precise nerve involved in the pain experienced by the patient. If an ilioinguinal nerve block ameliorates the patient's pain, a surgeon may conclude that electrical nerve stimulation is likely to be efficacious, and may proceed to surgically implant electrodes in accordance with the invention. Alternatively, a clinician may stimulate the patient using an insulated needle to determine the nerve involved and the placement of an electrode. The diagnosis may also be made using the results of the patient history, physical examination, and preoperative electromyography.

IMD 28 may be implanted at a site in patient 10 near ilioinguinal nerves 30 and 31. The implantation site may be a subcutaneous location in the side of the lower abdomen. Alternatively, IMD 28 may be implanted within the scrotum or buttock of the patient. IMD 28 may be miniaturized to allow IMD 28 to be implanted within the scrotum. In any case, the surgeon may then tunnel a lead through tissue and subsequently connect the lead to IMD 28, with or without a lead extension. IMD 28 may be constructed with a biocompatible housing, such as titanium or stainless steel, much like a conventional neurostimulator such as those used for spinal cord stimulation or pelvic stimulation, e.g., for relief of chronic pain, sexual dysfunction, or urinary or fecal incontinence.

External programmer 29 may control delivery of electrical stimulation by IMD 28. For example, in some embodiments, external programmer 28 may comprise a clinician programmer or a patient programmer. A clinician programmer may be a handheld computing device including a display, such as an LCD or LED display, to display electrical stimulation parameters. A clinician programmer may also include a keypad, which may be used by a user to interact with the clinician programmer. In some embodiments, the display may be a touch screen display, and a user may interact with the clinician programmer via the display. A user may also interact with the clinician programmer using peripheral pointing devices, such as a stylus or mouse. The keypad may take the form of an alphanumeric keypad or a reduced set of keys associated with particular functions.

A clinician (not shown) may use the clinician programmer to program electrical stimulation to be delivered to patient 10. In particular, the clinician may use the clinician programmer to select values for therapy parameters, such as pulse amplitude, pulse width, pulse rate, electrode polarity and duty cycle, for one of or both electrodes 16 and 17. IMD 28 may deliver the electrical stimulation according to programs, each program including values for a plurality of such therapy parameters. In this manner, IMD 28 controls delivery of electrical stimulation according to preprogrammed stimulation programs and schedules.

When implemented as a patient programmer, external programmer 29 may be a handheld computing device. The patient programmer 26 may also include a display and a keypad to allow patient 10 to interact with the patient programmer. In some embodiments, the display may be a touch screen display, and patient 10 may interact with the patient programmer via the display. Patient 10 may also interact with the patient programmer using peripheral pointing devices, such as a stylus or mouse.

Patient 10 may use the patient programmer to control the delivery of electrical stimulation. In particular, in response to a command from patient 10, external programmer 29 may activate IMD 28 to deliver electrical stimulation or, alternatively, deactivate IMD 28 when no electrical stimulation is desired. Patient 10 may also use the patient programmer to select the programs that will be used by IMD 28 to deliver electrical stimulation. Further, patient 10 may use the patient programmer to make adjustments to programs, such as adjustments to amplitude, pulse width and/or pulse rate. Additionally, the clinician or patient 10 may use a clinician or patient programmer to create or adjust schedules for delivery of electrical stimulation.

IMD 28 and external programmer 29, implemented as a clinician programmer or a patient programmer, communicate via wireless communication. In some embodiments, external programmer 29 communicates via wireless communication with IMD 28 using radio frequency (RF) telemetry techniques known in the art. The clinician programmer and patient programmer may communicate with one another by wireless communication, e.g., to change or update programs. Alternatively, the programmers may communicate via a wired connection, such as via a serial communication cable, or via exchange of removable media, such as magnetic or optical disks, or memory cards.

As previously described, leads 18 and 19 may be implanted surgically or percutaneously. When inserted percutaneously, leads 18 and 19 may be used in conjunction with an external trial stimulator (not shown) in order to determine if permanent implantation of the electrodes and leads is an effective treatment for the patient's pain. For example, prior to implantation of IMD 28, patient 10 may engage in a trial period, in which patient 10 receives an external trial stimulator on a temporary basis. The external trial stimulator may be coupled to temporary leads or chronically implanted leads via a percutaneous lead extension.

The trial neurostimulation permits a clinician to observe neurostimulation efficacy and determine whether implantation of a chronic neurostimulation device is advisable. Specifically, the trial neurostimulation period may assist the clinician in selecting values for a number of programmable parameters in order to define the neurostimulation therapy delivered to patient 10. For example, the clinician may select an amplitude, which may be current- or voltage-controlled, and pulse width for a stimulation waveform to be delivered to patient 10, as well as a rate, i.e., frequency) delivered to the patient. In addition, the clinician also selects particular electrodes on a lead to be used to deliver the pulses, and the polarities of the selected electrodes.

By stimulating ilioinguinal nerves 30 and 31, a system in accordance with an embodiment of the invention may substantially reduce or eliminate pelvic pain such as chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term pain in the testicles, groin, or abdomen. Ilioinguinal denervation procedures may result in permanent and substantial pain relief but may also cause unwanted side effects, such as loss of sensation in the skin of the superomedial thigh, penis, testicle and/or scrotum. Therapeutic nerve blocks may also be used to treat ilioinguinal neuralgia, but generally only relieve pain temporarily. Because electrical stimulation does not require severing the ilioinguinal nerves cord and, more particularly, aims to avoid damaging nerves, the invention may provide similar or improved pain relief without the unwanted side effects.

FIG. 2 is a schematic diagram further illustrating system 2. In particular, system 2 is illustrated from the left side of patient 10. For purposes of illustration, only spermatic cord 15, external fascia layer 35, genital nerve branch 23, inguinal canal 27, ilioinguinal nerve 31, testicle 13, and scrotal area 11 are shown. In FIG. 2, cuff electrode 16 is illustrated as being wrapped around a portion of ilioinguinal nerve 31 below inguinal canal 27 to illustrate the different locations at which electrodes may be implanted and to illustrate an embodiment in which multiple electrodes are implanted along a single spermatic cord 15. Accordingly, an additional cuff electrode 17 is shown as being wrapped around genital nerve branch 23, while cuff electrode 16 is shown as being wrapped around a different portion of ilioinguinal nerve 31 above inguinal canal 27.

In an embodiment in which two or more electrodes are implanted along the same ilioinguinal nerve 31, the electrodes may form a bipolar pair that is referenced between two electrodes deployed by leads 18, 19, or be individually referenced to an electrical potential associated with an electrode on the housing of IMD 28. Also, in some embodiments, multiple cuffs or leads may be implanted along a single ilioinguinal nerve 31, and each may carry multiple electrodes, e.g., in an axial or planar array, providing still more possible electrode combinations for selection by a physician. In addition, one or more electrodes may be deployed to stimulate one or both ilioinguinal nerves 30, 31, as described with reference to FIG. 1.

FIG. 2 illustrates ilioinguinal nerve 31 passing through inguinal canal 27 to innervate penis 8, scrotum 11, and the skin of the superomedial thigh (not shown) of patient 10. In particular, ilioinguinal nerve 31 is illustrated in FIG. 2 as entering inguinal canal 27 from the side rather than passing through the deep (internal) inguinal ring and exits inguinal canal through the superficial (internal) inguinal ring. In some cases, branches of ilioinguinal nerve 31 may innervate spermatic cord 15. Genital nerve branch 23 originating from genitofemoral nerve 21 and passing through inguinal canal 27 to innervate testicle 13 is also shown. As previously described, spermatic cord 15 joins an external fascia layer 35 as it passes through the superficial ring of inguinal canal 27.

Cuff electrode 16 is wrapped around a portion of ilioinguinal nerve 31 below inguinal canal 27, i.e., a portion of ilioinguinal nerve 31 after exiting inguinal canal 27. Optionally, another electrode is provided. For example, cuff electrode 17 is wrapped around a portion of ilioinguinal nerve 31 above inguinal canal 27, i.e., a portion of ilioinguinal nerve 31 before entering inguinal canal 27. Because cuff electrode 17 is located higher (upstream in the central nervous system) from cuff electrode 16, patient 10 may experience parasthesia over a larger area, which may be advantageous in some instances.

In general, cuff electrodes 16 and 17 may be particularly advantageous because cuff electrodes 16 and 17 may remain in place as patient 10 moves without requiring any external fixation means such as sutures or anchoring mechanisms. External fixation means may damage tissue or the nerve itself, possibly causing additional pain which may reduce the efficacy of the electrical stimulation therapy. Cuff electrodes 16 and 17 include a fixation structure that at least partially wraps around ilioinguinal nerve 31. The fixation structure may be fabricated from a flexible biocompatible material that provides a flexible interface between the electrode and ilioinguinal nerve 31.

In some embodiments, the cuff fixation structure may be fabricated from a flexible or rigid biocompatible material. In such cases, the fixation structure may form a split cylinder or a “U” shape sized to fit around ilioinguinal nerve 31. Cuff electrodes 16 and 17 may generally comprise a rigid cuff electrode, a self-sizing spiral cuff electrode, a half cuff electrode, a helical electrode, a chambered electrode, and other types of cuff electrodes that at least partially wrap around one of ilioinguinal nerves 30 and 31. Upon enclosure of at least a portion of ilioinguinal nerves 30 and 31, a cuff may be held in a closed position by shape memory properties, sutures, interlocking tabs, surgical adhesive, crimping, or other fixation techniques or structures.

FIGS. 3A, 3B and 3C are schematic diagrams illustrating an exemplary embodiment of a cuff electrode 16. Cuff electrode 17 may be similarly constructed. Cuff electrodes 16 and 17 may be any type of cuff electrode used to deliver electrical stimulation. In some embodiments, cuff electrodes 16 and 17 may both comprise the same type of cuff electrode or may comprise different types of cuff electrodes. In any case, cuff electrode 16 is merely exemplary and should not be considered limiting of the invention as broadly embodied and described in this disclosure. The purpose of FIGS. 3A-C is to illustrate the implantation of cuff electrodes to deliver electrical stimulation to the ilioinguinal nerves.

FIG. 3A is a top view of cuff electrode 16. Cuff electrode 16 includes lead 18, fixation structure 40, a plurality of stimulation electrodes 48A-C, and a plurality of electrical conductors 46 within lead 18. In the example of FIG. 3A, cuff electrode 16 includes three electrodes 48A, 48B, 48C. In the illustrated example, electrodes 48A-C are arranged such that a major axis of each electrode extends laterally to the ilioinguinal nerve. In this manner, the length of each electrode may be wrapped about all or a portion of the circumference of the ilioinguinal nerve. The proximal end 44 of lead 18 is connected to IMD 28 and fixation structure 40 is attached to the distal end 42 of lead 18. Cuff electrode 16 may generally include one electrode or a plurality of electrodes.

Each of electrodes 48A-C is coupled to one of a plurality of supply conductors 46. Electrodes 48A-C may be driven together via a common conductor or independently via separate conductors. When electrodes 48A-C are driven by a common conductor, they may be referenced to one or more electrodes carried by another lead or one or more electrodes carried by the IMD housing. When electrodes 48A-C are driven by separate conductors, bipolar or multipolar electrode combinations may be formed on a single lead or among two or more leads, as well as between one or more leads and the IMD housing.

For a given bipolar pair of electrodes on a lead, one supply conductor sources stimulation energy to a first electrode and a second supply conductor sinks stimulation energy from a second electrode, with the stimulation energy propagating across nerve tissue between the first and second electrodes. Hence, one electrode may form a cathode while the other forms an anode. Also, in some embodiments, multiple anodes and cathodes may be used in an electrode combination. A switch device in the IMD determines which electrodes will function as anodes and which electrodes will function as anodes.

As previously described, fixation structure 40 may be fabricated from a flexible biocompatible material that provides a flexible interface between the electrode and the ilioinguinal nerve. In some embodiments, fixation structure 40 may be fabricated from a rigid biocompatible material. The rigid fixation structure may form a split cylinder or a “U” shape sized to fit around the ilioinguinal nerve. In any case, when implanting electrode 16, the surgeon may elevate the ilioinguinal nerve and wrap fixation structure 40 around the ilioinguinal nerve.

The manner in which the surgeon installs the cuff electrode around the ilioinguinal nerve depends on the type of cuff electrode. For example, if fixation structure 40 is fabricated from a shape memory alloy, fixation structure 40 may recover its shape at a fixed temperature, e.g., slightly under room temperature. By sufficiently cooling fixation structure 40, the surgeon can easily open the cuff and position fixation structure 40 under the ilioinguinal nerve. Because the nominal body temperature of the patient is above room temperature, fixation structure 40 warms up and recovers its initial shape thereby closing or wrapping fixation structure 40 around the ilioinguinal nerve. In another example, the fixation structure may be constrained in a flat manner using a surgical tool or hand and, when released, wraps around the nerve.

FIG. 3B is a cross sectional view of cuff electrode 16 implanted underneath ilioinguinal nerve 31. In the illustrated example, fixation structure 40 is flat thereby allowing the surgeon to easily position electrode 16 under ilioinguinal nerve 31. When fixation structure 40 is fabricated from a shape memory alloy material, the surgeon may cool fixation structure 40 prior to positioning fixation structure 40 to easily manipulate fixation structure 40 into the open configuration shown in FIG. 3B. The surgeon may then position fixation structure under ilioinguinal nerve 31. Fixation structure 40 will recover its initial shape, i.e., a substantially closed ring sized to fit around ilioinguinal nerve 31, as fixation structure warms up to its activation temperature.

FIG. 3C is a cross sectional via of cuff electrode 16 implanted and wrapped around ilioinguinal nerve 31. More specifically, FIG. 3C illustrates the shape of fixation structure 40 when it has returned to its initial shape in response to warming from the patient's body heat. In the illustrated example, a gap 49 may exist between ilioinguinal nerve 31 and fixation structure 40. The gap may be filled with tissue or fluids and may provide a buffer that prevents cuff electrode 16 from damaging ilioinguinal nerve 31. Alternatively, fixation structure 40 may be sized to wrap around ilioinguinal nerve 31 such that there is substantially no gap between fixation structure 40 and ilioinguinal nerve 31. In some embodiments, the fixation structure may be deployed used superelastic properties of a shape memory allow such as Nitinol. For example, the fixation structure may be constrained in a flat shape either manually or with a surgical took, and then released so that it wraps around the nerve.

FIG. 4 is a block diagram illustrating an example configuration of IMD 28. IMD 28 may apply electrical stimulation to ilioinguinal nerves 30 and 31 of patient 10 via electrodes, e.g., cuff electrodes 16 and 17, coupled to IMD 28 via leads 18 and 19, respectively. The configuration, type, and number of electrodes illustrated in FIG. 4 are merely exemplary. Leadless stimulators alternatively may be used instead of or in addition to leads 18, 19 and cuff electrodes 16, 17. A leadless stimulator does not generally include any elongated leads, and instead carries electrodes on a housing of the stimulator or on a structure such as a fixation device extending from the housing.

In the example of FIG. 4, electrodes 16 and 17 are electrically coupled to a therapy delivery module 52 via leads 18 and 19, respectively. Therapy delivery module 52 may, for example, include an output pulse generator coupled to a power source such as a battery and charge storage capacitor. Therapy delivery module 52 may deliver electrical stimulation pulses to patient 10 via one or both of electrodes 16 and 17 under the control of a processor 54.

Processor 54 controls therapy delivery module 52 to deliver electrical stimulation according to a selected parameter set stored in memory 50. Specifically, processor 54 may control circuit 52 to deliver electrical stimulation pulses with the amplitudes and widths, and at the rates specified by the programs of the selected parameter set. Processor 54 may also control circuit 52 to deliver each pulse according to a different program of the parameter set. Processor 54 may include a microprocessor, a controller, a digital signal processor (DSP), an application specific integrated circuit (ASIC), a field programmable gate array (FPGA), or any other equivalent integrated or discrete logic circuitry, or the like.

In some embodiments, memory 50 may store parameter sets 58 that are available to be selected by patient 10 for delivery of electrical stimulation. Memory 50 may also store schedules 56. Memory 50 may include any combination of volatile, non-volatile, fixed, removable, magnetic, optical, or solid state media, such as a random access memory (RAM), random access memory (ROM), CD-ROM, hard disk, removable magnetic disk, memory cards, non-volatile RAM (NVRAM), electrically programmable ROM (EEPROM), flash memory, and the like.

IMD 28 delivers stimulation according to preprogrammed stimulation parameters and, optionally, schedules stored in memory 50. Schedules 56 may define times for processor 54 to select particular parameter sets 58 and control therapy delivery module to delivery therapy according to that parameter set. A schedule 56 may cause electrical stimulation to be delivered via electrodes 16 and 17 at respective times, which may include simultaneous and/or alternate delivery. For example, stimulation may be activated, deactivated or altered for different times of the day, such as times during which the patient is awake or sleeping, or working or at rest. A clinician or patient may create, modify, and select schedules 56 using external programmer 29.

IMD 28 also includes a telemetry circuit 53 that allows processor 54 to communicate with external programmer 29, i.e., a clinician programmer or patient programmer. Processor 54 may receive programs to test on patient 10 from external programmer 29 via telemetry circuit 52 during programming by a clinician. Where IMD 28 stores parameter sets 58 in memory 50, processor 54 may receive parameter sets 58 from external programmer 29 via telemetry circuit 52 during programming by a clinician, and later receive parameter set selections made by patient 10 from external programmer 29 via telemetry circuit 52. Where external programmer 29 stores the parameter sets, processor 54 may receive parameter sets selected by patient 10 from external programmer 29 via telemetry circuit 52.

FIG. 5 is a block diagram illustrating an example patient or clinician programmer 71 that allows a patient or clinician to program electrical stimulation therapy for a patient. Patient 10 or a clinician may interact with a processor 60 via a user interface 62 in order to control delivery of electrical therapy as described herein. User interface 62 may include a display and a keypad, and may also include a touch screen or peripheral pointing devices as described above. Processor 60 may also provide a graphical user interface (GUI) to facilitate interaction with patient 10, as will be described in greater detail below. Processor 60 may include a microprocessor, a controller, a DSP, an ASIC, an FPGA, discrete logic circuitry, or the like.

Programmer 71 also includes a memory 64. In some embodiments, memory 64 may store parameter sets 68 that are available to be selected by patient 10 or a clinician for delivery of electrical stimulation. Memory 64 may also store schedules 66. Hence, parameter sets and schedules may be stored in IMD 28, programmer 71, or both. Programmer 71 also includes a telemetry circuit 70 that allows processor 60 to communicate with IMD 28, and, optionally, input/output circuitry 72 (e.g., wired or wireless I/O media) to allow processor 60 to communicate with another programmer.

Processor 60 may receive parameter set selections made by patient 10 or a clinician via user interface 62, and may either transmit the selection or the selected parameter set to IMD 28 via telemetry circuitry 70 for delivery of electrical stimulation according to the selected parameter set. Where programmer 71 stores parameter sets 68 in memory 64, processor 60 may receive parameter sets 68 from another programmer via input/output circuitry 72 during programming by a clinician. Circuitry 72 may include transceivers for wireless communication, appropriate ports for wired communication or communication via removable electrical media, or appropriate drives for communication via removable magnetic or optical media.

FIG. 6 is a schematic diagram illustrating another example system 100 for applying electrical stimulation to a male patient 10 for pelvic pain such as chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term (chronic) pain in the testicles, groin, or abdomen. System 100 also may be useful for alleviation of pelvic pain for female patients. In the illustrated example, system 100 includes electrodes 104 deployed on a lead extending from an IMD 108, and a leadless microstimulator 106. Electrodes 104 and leadless microstimulator 106 deliver electrical stimulation to ilioinguinal nerves 31 and 30, respectively, and illustrate alternative arrangements stimulation. Hence, stimulation energy may be delivered to ilioinguinal nerves 30, 31 via any combination of cuff electrodes, axial electrode arrays, planar electrode array (e.g., on paddle lead), leadless microstimulators, or other types of electrodes.

IMD 108 controls the delivery of electrical stimulation according to preprogrammed stimulation programs, parameter sets and/or schedules. In particular, IMD 108 or external programmer 109 may wirelessly control microstimulator 106 to deliver electrical stimulation to ilioinguinal nerve 30. Alternatively, microstimulator 106 may operate autonomously or in a coordinated manner in conjunction with other microstimulators or IMD 108. In the example of FIG. 6, IMD 108 is also coupled to electrodes 104 via lead 102. Again, the invention is not limited to the illustrated configuration. In general, IMD 108 may be coupled to any number and type of electrodes or electrical stimulators. The electrodes may also be positioned adjacent to one or both ilioinguinal nerves 30, 31 based on the perceived pain of patient 10. However, FIG. 7 illustrates example system 100 in which microstimulator 106 and electrodes 104 deliver bi-lateral electrical stimulation to ilioinguinal nerves 30 and 31, respectively.

In the illustrated example, microstimulator 106 is implanted adjacent to ilioinguinal nerve 30 and includes a housing and a fixation structure attached to the housing. The housing may be formed into a capsule-like shape and may be constructed from any of a variety of biocompatible materials, such as titanium or stainless steel. As will be described, the housing may carry an implantable pulse generator (IPG) and, optionally, a telemetry interface to exchange (send, receive or both) control signals with other devices such as IMD 108 or external programmer 109. The fixation structure on microstimulator 106 may be constructed similar to the fixation structure of previously described cuff electrodes 16 and 17. For example, the fixation structure on microstimulator 106 may be constructed of a flexible or a rigid biocompatible material that at least partially wraps around ilioinguinal nerve 30. The fixation structure may carry one or more electrodes, i.e., the electrodes may be integrated with the fixation structure, and the housing may include short leads that extend from the housing to couple the electrodes to the housing.

Alternatively, leadless microstimulator 106 may be implanted within tissue proximate or adjacent to ilioinguinal nerve 30 using a needle (not shown). In particular, microstimulator 106 may be implanted with a minimally invasive, percutaneous procedure. As an example, the needle may include a hollow cylinder and a pointed distal end for puncturing skin of patient 10. The needle may include the microstimulator and a fluid, e.g., saline solution, or push rod to force the microstimulator out of the needle. In this case, microstimulator 106 may be miniaturized in order to be implanted using the needle. In some embodiments, a plurality of microstimulators may be implanted within tissue proximate to the ilioinguinal nerve. The plurality of implanted microstimulators may apply electrical stimulation independently or on a coordinated basis.

When implanted within tissue proximate to ilioinguinal nerve 30, microstimulator 106 may comprise a self-contained module. The module comprises a housing that may carry one or more electrodes and an IPG within the housing. The IPG may comprise a circuit board and a power source, such as a battery, to provide power to the circuit board and electrodes. The circuit board may include the telemetry interface and other processing electronics. The electrodes may be pads mounted on a surface of the housing or ring electrodes that extend about the entire periphery of the housing. In some cases, the housing itself may form an active “can” electrode in addition to the electrodes mounted on the housing.

Microstimulator 106 may be implanted with less invasive procedures than other electrodes that are coupled to an IMD via a lead. For example, because microstimulator 106 may include a self-contained stimulation pulse generator and one or more electrodes, a surgeon does not have to tunnel a lead to IMD 108. In some embodiments, microstimulator 106 may wirelessly communicate with external programmer 109. In this case, external programmer 109 may be a small, battery-powered, portable device that may accompany patient 10 through the day. External programmer 109 may have a simple user interface, such as a button or keypad, and a display or lights. Patient 10 may only be able to activate and deactivate IMD 108. However, in other embodiments, external programmer 109 may include additional functionality to operate in a manner similar to a patient programmer.

In the illustrated example, ring electrodes 104 mounted on lead 102 also may be used to deliver electrical stimulation to ilioinguinal nerve 31. Lead 102 is coupled to IMD 108 and carries electrical conductors to transmit stimulation energy from the IMD to the electrodes 104 on a selective basis. In particular, one or more electrodes may be selected to form anodes and cathodes for delivery of stimulation energy via unipolar, bipolar or multipolar electrode combinations. Lead 102 may be implanted adjacent to ilioinguinal nerve 31 as shown. Lead 102 is shown in FIG. 6 carrying four electrodes, e.g., ring electrodes, although any number of electrodes could be used. Also, as mentioned previously, electrodes 104 may be arranged in an axial array, e.g., as ring electrodes, or in a two-dimensional planar array, e.g., in a paddle lead. Also, other types of leads providing curved or rounded electrode arrays may be used. At least one conductor is included in lead 102 that electrically connects the proximal end of lead 102 to electrodes 104 in its distal end. IMD 108 may control electrical stimulation applied by each of electrodes 104 separately or control electrical stimulation applied by a group of electrodes 104.

In some embodiments, lead 102 may be formed to include fixation elements, such as hooks, barbs, helical structures, tissue ingrowth mechanisms, or other anchoring mechanisms, e.g., at a distal end of lead 102. Fixation elements may serve to fix electrodes 104, relative to ilioinguinal nerve 31 so that electrodes 104 can provide consistent electrical simulation. Without anchoring electrodes 104 to ilioinguinal nerve 31 or tissue proximate to ilioinguinal nerve 31, the distance between electrodes 104 and spermatic cord may vary as patient 10 moves throughout the day, reducing the efficacy of the applied electrical stimulation. However, it is possible that anchoring mechanisms may damage the ilioinguinal nerve or surrounding tissue during implantation or as patient 10 moves.

System 100 generally operates in a similar manner to system 2 in FIG. 1 to apply electrical stimulation for chronic groin pain, ilioinguinal neuralgia, or other pelvic pain disorders. Accordingly, external programmer 109 may comprise a clinician programmer or a patient programmer. As shown, external programmer 109 may communicate via wireless communication with IMD 108. In particular, external programmer 109 may control delivery of electrical stimulation by IMD 108 using telemetry techniques known in the art. When microstimulator 106 comprises a self-contained module, external programmer 109 may directly communicate with microstimulator 106 via wireless communication to control delivery of electrical stimulation.

FIG. 7 is a schematic diagram further illustrating example system 100. In particular, system 100 is illustrated from the left side of a male patient 10 in FIG. 7. For purposes of illustration, only ilioinguinal nerve 31, genital nerve branch 23 of genitofemoral nerve 21, inguinal canal 27, testicle 13, scrotum 11, and penis 8 are shown. Again, ilioinguinal nerve 31 originates from the L1 and T12 and also, in some cases, the L2 nerve. Ilioinguinal nerve 31 innervates penis 8, scrotum 11, and the skin of the superomedial thigh (not shown). In some cases, branches of ilioinguinal nerve 31 may also innervate spermatic cord 15.

In general, electrical stimulation is applied to ilioinguinal nerve 31 through electrodes 104 of lead 102 implanted adjacent to ilioinguinal nerve 31. Electrodes 104 apply electrical stimulation to ilioinguinal nerve 31 under control of IMD 108. Lead 102 carries electrodes 104 and couples electrodes 104 to IMD 108. In particular, at least one electrical conductor is included in lead 102 that electrically connects electrodes 104 to IMD 108. Electrodes 104 may comprise four electrodes, e.g., ring electrodes, although the invention is not so limited. Electrodes 104 may comprise any number and type of electrodes. In some embodiments, as mentioned above, lead 102 also may include fixation elements, such as hooks, barbs, helical structures, tissue ingrowth mechanisms, or other anchoring mechanisms that aid in securing lead 102 to ilioinguinal nerve 31 or tissue proximate to ilioinguinal nerve 31. Securing lead 102 to ilioinguinal nerve 31 or to tissue proximate to ilioinguinal nerve 31 may prevent lead 102 from moving relative to ilioinguinal nerve 31.

IMD 108 is programmed to deliver electrical stimulation appropriate for chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term (chronic) pain in the testicles, groin, or abdomen. IMD 108 may control electrical stimulation applied by each of electrodes 104 independently. Alternatively, IMD 108 may control electrical stimulation applied by a group of electrodes 104, and may select different combinations of electrodes 104 in bipolar or multi-polar arrangements to identify a particular combination that is most effective in producing desired parasthesia. Again, IMD 108 may control delivery of electrical stimulation according to parameter sets and/or schedules programmed in internal memory.

Although FIG. 7 illustrates lead 102 implanted adjacent to ilioinguinal nerve 31 below inguinal canal 27, lead 102 may be implanted adjacent to ilioinguinal nerve 31 above inguinal canal 27. In this case, applying electrical stimulation to ilioinguinal nerve 31 at a location further upstream may cause patient 10 to experience a larger area of paresthesia in response to electrical stimulation. In both male and female patients, stimulation may be applied close or below the inquiry cancel 27.

FIGS. 8A and 8B show exemplary electrical leads with fixation elements to secure the lead within a patient. As shown in FIG. 8A, lead 110 includes lead body 112, tines 116A-D (collectively tines 116) and electrodes 114A-D (collectively electrodes 114). Lead 110 may be a standard lead that includes all four tines 116 close to electrodes 114. Lead 110 may be implemented with any number of electrodes or tines. When implanting lead 110, having tines 116 close to electrodes 114 may be beneficial by allowing less movement of electrodes 114 with respect to the spermatic cord.

Electrodes 114 are more effective in delivering electrical stimulation when the electrodes are located close to the ilioinguinal nerve. If electrodes 114 migrate away from the spermatic cord, due to movement of the patient throughout the day, for example, the efficacy of the stimulation may decrease. Therefore, tines 116 located close to electrodes 114 may be beneficial to therapy efficacy.

FIG. 8B illustrates a lead 120 which includes lead body 122, tines 126, and electrodes 124A-D (collectively electrodes 124). Lead 120 may be a standard lead that includes tines 126 located at the distal end of lead body 122. Lead 120 may be implemented with any number of electrodes or tines. Electrodes 124 may be located close to or a distance away from tines 126. When electrodes 124 are close to tines 126, implanting lead 120 may allow less movement of electrodes 124 with respect to the ilioinguinal nerve. Consequently, the intensity of electrical stimulation delivered to the ilioinguinal nerve may not vary and cause the patient to experience different levels of paresthesia.

When electrodes 124 are located a distance away from tines 126, implanting lead 102 may allow electrodes 124 to reach further away from the anchoring site. For example, when lead 102 delivers electrical stimulation to the ilioinguinal nerve above the inguinal canal, i.e., before the ilioinguinal nerve enters the inguinal canal, tines may be anchored to tissue a distance away from the ilioinguinal nerve while leads may be located proximate to the ilioinguinal nerve. Securing tines 126 to the ilioinguinal nerve is undesirable because the nerve may be damaged in the process. Thus, lead 120 may be beneficial by preventing unwanted nerve damage during the implantation process.

FIG. 9 is a schematic diagram further illustrating example system 100. In particular, system 100 is illustrated from the right side of a male patient 10. For purposes of illustration, only ilioinguinal nerve 30, genital nerve branch 22 of genitofemoral nerve 20, inguinal canal 26, testicle 12, scrotum 11, and penis 8 are shown. As previously described and similar to ilioinguinal nerve 31, ilioinguinal nerve 30 originates from the L1 and T12 and also, in some cases, the L2 nerve. Ilioinguinal nerve 31 innervates penis 8, scrotum 11, and the skin of the superomedial thigh (not shown). In some cases, branches of ilioinguinal nerve 31 may also innervate spermatic cord 14 which joins an external fascia layer 36 as it passes through the superficial ring of inguinal canal 26.

Microstimulator 106 applies electrical stimulation to ilioinguinal nerve 30 under control of IMD 108 or external programmer 109. As shown, IMD 108 or external programmer 109 may wirelessly control microstimulator 106 to delivery electrical stimulation. Microelectrode 106 includes a housing 107 and a fixation structure 105, such as a cuff, attached to housing 107. Housing 107 may be formed into a capsule-like shape and may be constructed from any of a variety of biocompatible materials, such as titanium. Housing 107 may carry an implantable pulse generator (IPG) and a telemetry interface to receive control signals from IMD 108. Fixation structure 105 wraps at least partially around ilioinguinal nerve 30 to secure microstimulator 106 in place. Accordingly, fixation structure 105 may operate and be constructed similar to the fixation structure of previously described cuff electrodes 16 and 17. Fixation structure 105 may carry one or more electrodes coupled to housing 107 via short leads (not shown). In some embodiments, housing 107 may form an active “can” electrode.

The invention is not limited to the illustrated configuration. For example, microstimulator 106 may also be implanted to deliver electrical stimulation to ilioinguinal nerve 30 above inguinal canal 26. In this case, fixation structure 105 wraps at least partially around ilioinguinal nerve 30. In addition, in some embodiments, a microstimulator may implanted to deliver electrical stimulation at both locations in a coordinated manner or independently of each other.

FIGS. 10A-10C are enlarged schematic diagrams showing microstimulator 106. In particular, FIG. 10A is an enlarged top view of microstimulator 106 including housing 107, circuit board 130, power supply 132, fixation structure 105, and electrodes 108A-C (collectively electrodes 108). Housing 107 may have a rounded, capsule-like shape, and a smooth, atraumatic surface formed of one or more biocompatible materials, such as titanium, stainless steel, epoxy, or polyvinylchloride. However, the invention is not so limited. Instead, housing 107 may have a shape that is compatible with the anatomy at the implant site, i.e., the ilioinguinal nerve before it enters the inguinal canal. In some embodiments, the leadless microstimulator may have a capsule shape with a diameter of approximately less than or equal to 2 cm and a length of less than or equal to approximately 5 cm.

Fixation structure 105 may be constructed of a flexible or rigid biocompatible material that at least partially wraps around the ilioinguinal nerve, e.g., like a cuff. For example, fixation structure 105 may be fabricated from a shape memory alloy that has the capacity to recover a memorized shape when deformed at a certain temperature and then heated at a higher temperature or vice versa. In this case, the memorized shape may be a split cylinder or a substantially closed cylinder with a diameter sized to wrap around the ilioinguinal nerve.

FIG. 10A illustrates fixation structure 105 in a deformed, generally open state that enables a surgeon to easily position slip microstimulator 106 underneath the ilioinguinal nerve. However, after positioning microstimulator 106 beneath the spermatic cord, the body temperature of the patient causes fixation structure 105 to recover its memorized shape, i.e., a split cylinder. Therefore, fixation structure 105 may be beneficial by reducing trauma during surgical implantation procedures.

Fixation structure 105 also carries one or more electrodes 108. Electrodes 108 may be driven together or independently. For example, electrodes 108 may be selectively driven to form combinations of anodes and cathodes. Electrodes 108 may be integrated with fixation structure 105 or, alternatively housing 107 may include short leads (not shown) that extend from housing 107 to couple electrodes 108 to housing 107.

Circuit board 130 may include a processor, memory, pulse generator circuitry to generate electrical pulses delivered by 108, and telemetry circuitry for wireless telemetry with IMD 108, external programmer 109, or both. As an example, the memory may store stimulation parameters, e.g., electrode polarity, pulse width, pulse rate, and amplitude. Memory may also store schedules which define times for the processor to select particular parameters. A schedule may cause electrical stimulation to be delivered at respective times. In this manner, the processor may control the pulse generator circuitry generate electrical stimulation pulses in accordance with the selected parameters and schedule.

Microstimulator 106 may also operate under control from an external programmer, so that a physician or patient may activate, deactivate and/or modify stimulation delivered to the patient on a selective basis. Power source 132 supplies operating power to circuit board 130 and may take the form of a small rechargeable or non-rechargeable battery. Different types of batteries or different battery sizes may be used. To promote longevity, power source 132 may be rechargeable via induction or other means.

FIG. 10B illustrates a cross sectional view of microstimulator 106 implanted underneath ilioinguinal nerve 30. In the illustrated example, fixation structure 105 is flat, thereby allowing the surgeon to easily position microelectrode 106 underneath ilioinguinal nerve 30. When fabricated from a shape memory alloy, the body temperature of patient 10 may heat fixation structure 105 above the recovery shape temperature. In another example, fixation structure 105 may be constrained in a flat manner using a surgical tool or hand and, when released, wraps around the nerve.

FIG. 10C is a cross sectional view of microelectrode 106 with fixations structure 105 wrapped substantially around ilioinguinal nerve 30. For example, as fixation structure 105 is warmed above its recovery shape temperature, fixation structure 105 recovers its initial shape, i.e., a substantially closed cylinder or ring. As shown in FIG. 10C, in some embodiments, fixation structure 105 may not close completely. However, fixation structure 105 may at least wrap partially around ilioinguinal nerve 30 in order to secure microstimulator 106 to the nerve site. Removing microelectrode 106 may be easier when fixation structure 105 does not completely wrap around ilioinguinal nerve 30 because the gap between the ends of fixation structure 105 may provide an area to insert a tool that aids in removal. In alternative embodiments, fixation structure 105 may wrap completely around ilioinguinal nerve 30.

In the illustrated example, a gap 111 exists between ilioinguinal nerve 30 and fixation structure 105. Gap 111 may be filled with tissue or fluids and may provide a buffer that prevents microstimulator 106 from damaging ilioinguinal nerve 30. Alternatively, fixation structure 105 may be sized to wrap around ilioinguinal nerve 30 such that there is substantially no gap between fixation structure 105 and ilioinguinal nerve 30.

FIG. 11 is cross-sectional view of a microstimulator 140 implanted within, for example, tissue 141 proximate or adjacent to ilioinguinal nerve 30. Housing 142 of microstimulator 140 is embedded in tissue 141 proximate to ilioinguinal nerve 30 and includes circuit board 144, power source 146, and electrodes 148 and 149. Housing 142 is in the shape of a rounded capsule and includes a smooth surface. The only structure extending from housing 142 are electrodes 148 and 149. Electrodes 148 and 149 may protrude slightly from housing 142 or, alternatively, may be integrated into housing 142 to apply electrical stimulation to tissue 141. Electrodes 148 and 149 may be constructed as pads, as shown in FIG. 11, or as ring electrodes, as shown in FIG. 12. Microstimulator 140 rests in wall cavity 150 formed within external fascia 141. As previously described, microstimulator 140 may have a cylindrical shape with a diameter of less than or equal to approximately 2 cm and a length of less than or equal to approximately 5 cm.

Circuit board 144, power source 146, and electrodes 148 and 149 may be similar to respective circuit board 130, power source 132, and electrodes 108 of FIGS. 11A-C. Differences between these components of each embodiment may relate to the size or shape of each component. Therefore, electrodes 148 and 149 apply electrical stimulation under control of circuit board 144. Power source supplies operating power to circuit board 144. Circuit board 144 may select may select stimulation parameters and cause electrodes 148 and 149 to apply electrical pulses with the selected parameters according to schedules stored in memory. Circuit board 140 receives control signals from IMD 108, external programmer 109, or both by wireless telemetry. In some embodiments, one of electrodes 148 and 149 may comprise a sensor or microstimulator 140 may additionally include a sensor that detects a physiological parameter. In such embodiments, the sensor may sense a change in a physiological parameter. Processing electronics on circuit board 144 detects the change and causes electrodes to apply electrical stimulation in response to the change.

Implanting microstimulator 140 within tissue 141 proximate to ilioinguinal nerve 30 may be a simple method for securing electrodes 148 and 149. In some embodiments, a plurality of microstimulators similar to microstimulator 140 may be implanted and apply electrical stimulation to ilioinguinal nerve 30 in a coordinated manner or in a manner independent of each other.

FIG. 12 is a schematic diagram illustrating implantation of microstimulator 140 within tissue 141 of ilioinguinal nerve 30. Microstimulator 140 may be implanted through endoscopic, laparoscopic, or similar minimally invasive techniques. A surgeon may make a small inguinal incision in patient 10 and guides microstimulator 140 within needle 152 to tissue 141. Needle 152 may be constructed of a metal alloy and comprise a hollow cylinder and a pointed distal end for puncturing the skin of patient 10. Needle 152 includes microstimulator 140 and a fluid or push rod to force microstimulator 140 out of the needle. An exemplary fluid may be saline or other biocompatible fluid.

Once needle 152 in positioned at the appropriate location with respect to ilioinguinal nerve 30, the surgeon may force microstimulator 140 into place. Removing needle 152 from tissue 141 proximate to ilioinguinal nerve 30 allows tissue 141 to close and surround microstimulator 140. When implanting microstimulator 140, tissue 141 should not be breached in order to prevent ilioinguinal nerve 30 from being damaged.

In other embodiments, microstimulator 140 may be implanted through more invasive procedures which expose ilioinguinal nerve 30. As previously described, multiple microstimulators may be implanted in tissue 141 proximate to ilioinguinal nerve 30 to apply electrical stimulation to a larger area.

FIG. 13 is a functional block diagram illustrating various components of an example microstimulator 106 (FIG. 6) or microstimulator 140 (FIG. 11). In the example of FIG. 9, microstimulator 140 includes a processor 160, memory 162, pulse generator circuitry 164, telemetry interface 168, power source 166 and electrodes 165. Pulse generator circuitry 164 may be carried on a circuit board, along with processor 160, memory 162, and telemetry interface 168. Memory 162 may store instructions for execution by processor 160, stimulation parameters, e.g., electrode polarity, pulse width, pulse rate, and amplitude, and schedules for delivering electrical stimulation. Memory 162 may include separate memories for storing instructions, stimulation parameter sets, and schedules. Memory 162 may comprise any form of computer-readable media such as magnetic or optical tape or disks, solid state volatile or non-volatile memory, including random access memory (RAM), read only memory (ROM), electronically programmable memory (EPROM or EEPROM), or flash memory.

Processor 160 controls pulse generator circuitry 164 to deliver electrical stimulation via electrodes 165. Electrodes 165 may comprise any number and type of electrodes previously described, i.e., electrodes 108 (FIG. 6) and electrodes 148 and 149 (FIG. 11). An exemplary range of stimulation pulse parameters likely to be effective in treating post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term pain in the testicles, groin, or abdomen when applied to the ilioinguinal nerve are as follows: pulse widths between approximately 10 and 5000 microseconds, more preferably between approximately 100 and 1000 microseconds and still more preferably between 180 and 450 microseconds; voltage amplitudes between approximately 0.1 and 50 volts, more preferably between approximately 0.5 and 20 volts and still more preferably between approximately 1 and 10 volts; and frequencies between approximately 0.5 and 500 hertz, more preferably between approximately 10 and 250 hertz and still more preferably between approximately 50 and 150 hertz. The pulses may be alternating current (ac) pulses or direct current (dc) pulses, and may be mono-phasic, bi-phasic, or multi-phasic in various embodiments.

Processor 160 also controls telemetry interface 168 to receive information from IMD 108, external programmer 109, or both. Telemetry interface 168 may communicate via wireless telemetry, e.g., RF communication, on a continuous basis, at periodic intervals, or upon request from the implantable stimulator or programmer. Processor 160 may include a single or multiple processors that are realized by microprocessors, Application-Specific Integrated Circuits (ASIC), Field-Programmable Gate Arrays (FPGA), or other equivalent integrated or discrete logic circuitry.

Power source 166 delivers operating power to the components of the implantable microstimulator. As mentioned previously, power source 166 may include a small rechargeable or non-rechargeable battery and a power generation circuit to produce the operating power.

FIG. 14 is a schematic diagram illustrating another configuration for example system 100 of FIG. 7. In particular, rather than being implanted along ilioinguinal nerve 31, electrodes 104 are illustrated in FIG. 14 as being implanted perpendicular to ilioinguinal nerve 31. Implanting electrodes 104 perpendicular to ilioinguinal nerve 31 may provide certain advantages. For example, when implanted as shown, electrodes 104 may more effectively apply electrical stimulation to a point along ilioinguinal nerve 31 instead of applying electrical stimulation along a length or portion of ilioinguinal nerve 31. Patient 10 may experience a more complete relief of pain or fewer unwanted side effects as a result of applying electrical stimulation in this manner. The invention is not limited to the illustrated embodiments. Instead, electrodes 104 may be implanted at any orientation with respect to ilioinguinal nerve 31.

FIG. 15 is a flow chart illustrating a technique for applying electrical stimulation to an ilioinguinal nerve of a patient using an implantable electrode. Any of the previously described electrodes, i.e., cuff electrodes 16 and 17 (FIG. 1), electrodes 104 carried by lead 102 (FIG. 6), microstimulator 106 (FIG. 6), and microstimulator 140 (FIG. 11), may be implanted in accordance with the steps of the illustrated flow chart. The flow of events begins with the surgical procedure for implanting the electrode. The surgical procedure for exposing the ilioinguinal nerve for lead placement is well defined and may be used. Specifically, the surgeon makes an inguinal incision (170) as used for standard ilioinguinal denervation or hernia repair.

The surgeon identifies the ilioinguinal nerve (172) and implants an electrode adjacent to the ilioinguinal nerve (174). When implanting a cuff electrode, the surgeon may elevate the ilioinguinal nerve and wrap the cuff electrode around the ilioinguinal nerve. If the fixation structure of the cuff electrode is formed from a shape memory alloy, the body temperature of the patient may cause the fixation structure to recover its initial shape, i.e., a substantially closed cylinder or ring shape sized to fit around the ilioinguinal nerve. In any case, the cuff electrode may wrap at least partially around the ilioinguinal nerve thereby securing the cuff electrode to the ilioinguinal nerve.

When implanting lead 102 carrying electrodes 104, fixation elements such as hooks, barbs, helical structures, tissue ingrowth mechanisms, or other anchoring mechanisms may secure lead 102 to the ilioinguinal nerve or tissue proximate to the ilioinguinal nerve. Leads carrying electrodes may provide distinct advantages due to the number of electrodes available to apply electrical stimulation. For example, leads are available that carry eight, sixteen, or more electrodes which can be used to apply electrical stimulation in various groups or independently of each other. Further, because the electrodes may be positioned along a substantial length of the lead, the electrodes may apply electrical stimulation along a larger area of the ilioinguinal nerve.

The surgeon may implant microstimulator 106 similar to cuff electrodes 16 and 17 because the fixation structure of microstimulator 106 may operate in the same manner as the fixation structure of cuff electrodes 16 and 17. In contrast, the surgeon may implant microstimulator 140 within tissue proximate or adjacent to the ilioinguinal nerve using a needle. The needle may comprise a hollow cylinder and a pointed distal end for puncturing the skin of the patient and a fluid to force microstimulator 140 out of the needle. Accordingly, the surgeon may not need to make an inguinal incision when implanting microstimulator 140 within the tissue proximate to the ilioinguinal nerve. Rather, once the needle is positioned at the appropriate location with respect to the ilioinguinal nerve, the surgeon forces microstimulator 140 into place by depressing the plunger of the needle thereby forcing the fluid and microstimulator out of the needle.

Removing the needle from the tissue allows the tissue to close and surround microstimulator 140. Consequently, microstimulator 140 may be implanted with a minimally invasive surgical procedure. Additionally, in some embodiments, the surgeon may implant a plurality of microstimulators along the ilioinguinal nerve. The microstimulators may provide electrical stimulation independently or on a coordinated basis.

In general, the implantation techniques may be used to implant electrodes proximate to a region of the inguinal nerve above or below the inguinal canal, i.e., a portion of ilioinguinal nerve prior to entering the inguinal canal or after exiting the inguinal canal. Implanting an electrode proximate to a region of the ilioinguinal nerve above the inguinal canal may provide paresthesia to a larger area of the patient because electrical stimulation is applied further upstream of the central nervous system (CNS).

In any case, after implanting the electrode, the surgeon may create a subcutaneous pocket in the abdomen of the patient (176) and implant an IMD, such as IMD 28 (FIG. 1) or IMD 108 (FIG. 6), within the subcutaneous pocket (178). In some embodiments, the IMD may be miniaturized and implanted within the scrotum of the patient. The surgeon may then tunnel the electrode lead through the tissue in the patient to the implantation site and connect the lead to the implanted electrode(s) (180). Notably, microstimulators 106 and 140 may wirelessly communicate with external programmer 109 to receive control signals and, thus, not require an IMD.

When the surgical implantation procedure is complete, the implanted electrodes may apply electrical stimulation to deliver therapy (182) the ilioinguinal nerve. Applying electrical stimulation to the ilioinguinal nerve may block pain signals from the penis, testicles, and the associated scrotal area from reaching the CNS. The pain experienced by the patient may be uni-lateral or bi-lateral. Consequently, electrodes may be implanted adjacent to one or both ilioinguinal nerves of a patient. The pain experienced by the patient may also be constant or intermittent, or spontaneous or exacerbated by physical activities and pressure. Thus, the implanted electrodes may apply electrical stimulation on demand, such as in response to a control signal received from a patient or clinician programmer, or in accordance with preprogrammed cycles or schedules.

Electrical stimulation of the ilioinguinal nerve may provide may provide substantial relief of pelvic pain experienced by male and female patients, including urogenital pain or other forms of pelvic pain. In male patients, for example, electrical stimulation of the ilioinguinal nerve may relieve a variety of pelvic pain conditions such as chronic groin pain, post vasectomy pain, ilioinguinal neuralgia, and other conditions that cause long term (chronic) pain in the testicles, groin, or abdomen. For female patients, electrical stimulation of the ilioinguinal nerve may alleviate a variety of pelvic pain conditions such as pain resulting from surgical procedures, vulvodynia, interstitial cystitis (painful bladder syndrome), adhesions, endometriosis, and pelvic congestion. Accordingly, although the invention has been primarily described with respect to male patients, the invention is not so limited and may be readily applied to female patients for similar relief of pain symptoms.

Many embodiments of the invention have been described. Various modifications may be made without departing from the scope of the claims. These and other embodiments are within the scope of the following claims. 

1. A method comprising: applying electrical stimulation, by an implantable electrical stimulation device, to at least a portion of a first ilioinguinal nerve via an electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point prior to the first ilioinguinal nerve entering a first inguinal canal of a patient; and applying electrical stimulation, by the implantable electrical stimulation device, to at least a portion of a second ilioinguinal nerve of the patient, wherein the implantable electrical stimulation device applies electrical stimulation to at least the portion of the first ilioinguinal nerve and to at least the portion of the second ilioinguinal nerve to alleviate pelvic pain.
 2. The method of claim 1, wherein applying electrical stimulation to at least the portion of the second ilioinguinal nerve of the patient comprises applying electrical stimulation to at least the portion of the second ilioinguinal nerve via a second electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point after the second ilioinguinal nerve exits a second inguinal canal of the patient.
 3. The method of claim 1, wherein the pelvic pain includes at least one of chronic groin pain, chronic testicular pain (CTP), post vasectomy pain, ilioinguinal neuralgia, vulvodynia, and interstitial cystitis.
 4. The method of claim 1, wherein the electrode includes at least one of a cuff electrode, a ring electrode, a planar electrode or an electrode on a leadless stimulator.
 5. The method of claim 1, wherein the electrode includes a cuff electrode including a cuff-like fixation structure and one or more electrodes.
 6. The method of claim 5, wherein the cuff electrode is mounted to an implantable medical lead coupled to the implantable electrical stimulation device.
 7. The method of claim 5, wherein the implantable electrical stimulation device includes a leadless stimulator, and the cuff electrode is mounted to the leadless stimulator.
 8. The method of claim 1, wherein the implantable electrical stimulation device includes a leadless stimulator sized for at least partial implantation within tissue proximate to the first ilioinguinal nerve of the patient.
 9. A method comprising: applying electrical stimulation, by an implantable electrical stimulation device, to at least a portion of a first ilioinguinal nerve via an electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point after the first ilioinguinal nerve exits a first inguinal canal of a patient; and applying electrical stimulation, by the implantable electrical stimulation device, to at least a portion of a second ilioinguinal nerve of the patient, wherein the implantable electrical stimulation device applies electrical stimulation to at least the portion of the first ilioinguinal nerve and to at least the portion of the second ilioinguinal nerve to alleviate pelvic pain.
 10. The method of claim 9, wherein applying electrical stimulation to at least the portion of the second ilioinguinal nerve of the patient comprises applying electrical stimulation to at least the portion of the second ilioinguinal nerve at a point after the second ilioinguinal nerve exits a second inguinal canal of the patient.
 11. The method of claim 9, wherein the electrical stimulation device delivers electrical stimulation selected to alleviate at least one of chronic groin pain, chronic testicular pain (CTP), post vasectomy pain, ilioinguinal neuralgia, vulvodynia, and interstitial cystitis.
 12. The method of claim 2, wherein the implantable electrical stimulation device applies electrical stimulation to the portion of the first ilioinguinal nerve and to the portion of the second ilioinguinal nerve on an interleaved basis, wherein the interleaved basis is based on a different pulse rate, duty cycle, or scheduled time for delivery of applied electrical stimulation.
 13. The method of claim 1, wherein applying electrical stimulation to at least the portion of the first ilioinguinal nerve comprises applying electrical stimulation to a first portion of the first ilioinguinal nerve, and wherein the method further comprises applying electrical stimulation to at least a second portion of the first ilioinguinal nerve via a second electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point after the first ilioinguinal nerve exits the first inguinal canal of the patient.
 14. The method of claim 13, wherein the implantable electrical stimulation device applies electrical stimulation to the first portion of the first ilioinguinal nerve and to the second portion of the first ilioinguinal nerve on an interleaved basis, wherein the interleaved basis is based on a different pulse rate, duty cycle, or scheduled time for delivery of applied electrical stimulation.
 15. A method comprising: applying electrical stimulation, by an implantable electrical stimulation device, to at least a portion of a first ilioinguinal nerve via an electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point prior to the first ilioinguinal nerve entering a first inguinal canal of a patient; and applying electrical stimulation, by the implantable electrical stimulation device, to at least a portion of a second ilioinguinal nerve of the patient, wherein the implantable electrical stimulation device applies electrical stimulation to at least the portion of the first ilioinguinal nerve and to at least the portion of the second ilioinguinal nerve on an interleaved basis to alleviate pelvic pain, wherein the interleaved basis is based on a different pulse rate, duty cycle, or scheduled time for delivery of applied electrical stimulation.
 16. A method comprising: applying electrical stimulation, by an implantable electrical stimulation device, to at least a portion of a first ilioinguinal nerve via an electrode that is coupled to the implantable electrical stimulation device and that is positioned at a point after the first ilioinguinal nerve exits a first inguinal canal of a patient; and applying electrical stimulation, by the implantable electrical stimulation device, to at least a portion of a second ilioinguinal nerve of the patient, wherein the implantable electrical stimulation device applies electrical stimulation to at least the portion of the first ilioinguinal nerve and to at least the portion of the second ilioinguinal nerve on an interleaved basis to alleviate pelvic pain, wherein the interleaved basis is based on a different pulse rate, duty cycle, or scheduled time for delivery of applied electrical stimulation. 